Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37780 | A02 | 32295009 | C | T | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S12 |
2 | BAA02g37780 | A02 | 32296651 | C | T | missense_variant | MODERATE | c.77C>T|p.Ser26Phe |
S152 |
3 | BAA02g37780 | A02 | 32297081 | C | T | synonymous_variant | LOW | c.277C>T|p.Leu93Leu |
S284 |
4 | BAA02g37780 | A02 | 32297220 | C | T | missense_variant | MODERATE | c.416C>T|p.Ser139Phe |
S173 |
5 | BAA02g37780 | A02 | 32297381 | C | T | missense_variant | MODERATE | c.488C>T|p.Ser163Leu |
S226 |
6 | BAA02g37780 | A02 | 32301799 | C | T | downstream_gene_variant | MODIFIER | c.*4216C>T| |
S165 |
7 | BAA02g37780 | A02 | 32302026 | C | T | downstream_gene_variant | MODIFIER | c.*4443C>T| |
S61 |
8 | BAA02g37780 | A02 | 32302397 | T | A | downstream_gene_variant | MODIFIER | c.*4814T>A| |
S176 |